The title compound, C(6)H(5)Cl(2)N, is almost planar, with an r.m.s. deviation of 0.0146 Å for all atoms except for the 5-choloromethyl Cl atom. The offset Cl atom lies above this plane with a Cl-C-C angle of 111.11 (17)°. In the crystal, mol-ecules are connected via inter-molecular C-H⋯N hydrogen bonds, forming dimers.

The synthesis of a new yellow fluorescent 4-(2-methylamino)-ethyloxy-N-PAMAM-1,8-naphthalimide from zero generation has been described. The chemical structure of synthesized dendrimers was confirmed using FT-IR, 1HNMR and DSC techniques. The new materials are comprised of a 1,8-naphthalimide fluorophore having a substituent at C-4 position. The synthesized compounds (P2 and P3) were ...

Z. Naturforsch. 54 b, 13-17 (1999); received June 1, 1998 Pyridine, 2-Silyl-pyridine, 2-Germyl-pyridine, 2-Stannyl-pyridine, Molecular Structure 5-Methyl-2-trimethylsilyl-pyridine (1) has recently been prepared via the “in situ” Grignard reaction of 1-bromo-5-methyl-pyridine with magnesium and trimethylchlorosilane in refluxing tetrahydrofuran (thf) and structurally characterized. 2-Trimethylge...

The title compound, C(6)H(8)N(3) (+)·Cl(-)·H(2)O, crystallizes with three formula units in the asymmetric unit. The cations are non-planar with the -C(NH(2))(2) groups twisted out of the ring planes. Each pyridine carboximidamidate cation is linked to another cation through N-H⋯N hydrogen bonds, to chloride ions by N-H⋯Cl hydrogen bonds, and to water mol-ecules by N-H⋯O hydrogen bonds. Water mo...

Many hands make light work: In an organocatalytic asymmetric sulfonation of enones, the activation of a sulfonyl imine by an N-heterocyclic carbene (NHC) catalyst led to the release of a sulfinic anion, which underwent nucleophilic addition to the enone. The enantioselectivity of the process was controlled by a chiral thiourea/amine co-catalyst through anion recognition and hydrogen-bonding int...